ACRE advice: New techniques used in plant breeding Executive summary Over recent years the number of enquiries has increased as to whether organisms produced by certain techniques are captured by the EU’s GMO legislation. In this advice, ACRE considers techniques that were identified by an EU Commission working group as posing particular challenges (these are listed in the first column of Table 1). ACRE has discussed these techniques in the context of plant breeding although many of them (or equivalents) are used in the modification of other organisms such as animals and microorganisms. We have come to our conclusions about the status of these techniques and the organisms that they generate by determining whether the scientific terms in the definition apply in each case. However, as the legal significance of many of these terms is not clear, Ministers will need to seek a legal opinion on our conclusions. Our considerations have highlighted three main issues where legal clarification is required. These issues are as follows. A. Are the offspring of GMOs necessarily GMOs? The answer may affect our conclusion on the status of organisms produced by reverse breeding. B. It is not clear what 'altering the genetic material of an organism in a way that does not occur naturally by mating or natural recombination' means in the context of this legislation. Does it require the formation of new combinations of genetic material that do not occur naturally, as may be implied by the examples of GM techniques in Part 1 of Annex 1A in Directive 2001/18/EC? In which case, it would not include modifications that do not alter the nucleotide sequence of the genetic material, or changes that will result in nucleotide sequences that are likely to be present in nature or as a result of conventional breeding. This fundamental question has ramifications for other issues linked to interpreting the definition. In particular, the answer may affect our conclusions on cisgenics and RNA-dependent DNA methylation. C. ACRE contests the relevance of referring to ‘recombinant nucleic acid molecules’ where these molecules are not inserted into the genome of the host organism i.e. in Annex 1B of Directive 2001/18/EC, which lists GM techniques that produce 1 organisms that are excluded from the legislation. This point is relevant to our conclusion on the status of organisms produced by mutation, such as through the use of zinc finger nucleases or oligonucleotides. Table 1 summarises ACRE’s conclusions on the status of these techniques and the organisms generated by them. We note that a combination of these techniques may be used in the generation of a new plant variety. The asterisks in Table 1 indicate where there is flexibility in the legal interpretation of the definition that could affect ACRE’s conclusions. The three issues listed above are the source of this uncertainty; the letters in brackets in Table 1 relate to this list. This uncertainty is discussed in more detail in the respective sections of the report. The techniques that require a decision as to the regulatory status of their products most urgently are cisgenesis and oligo-directed mutagenesis. 1 Techniques Involves a GM Produces an Offspring are technique? intermediate product GMOs? that is a GMO? Cisgenesis/intragenesis Yes*(B)/Yes - Yes*(B)/Yes Reverse breeding Yes Yes No2* (A) Agroinfiltration Yes questionable3 No2 Grafting (non-GM scion/GM No Yes No rootstock) RNA-dependent DNA No - nucleic acid No No*(B) methylation molecules not inserted into genome. Yes – nucleic acid Yes No2*(B) 1 Produced by sexual reproduction. 2 Generally a technique that involves the insertion of nucleic acid molecules into the host plant‟s genome would be considered a GM technique (noting our question about the need to form new combinations of genetic material). Intermediate products containing this genetic material would be considered GMOs. However, offspring that do not contain this inserted material would not be considered GMOs. 3 Questionable but not significant to regulators in this context because the plants are containers for GM Agrobacterium and this will need to be regulated anyway. It is significant in the context of animals vaccinated with DNA vaccines – but this is not discussed here because it raises further issues about continued propagation/ heritability of the genetic modification. 2 molecules inserted into genome Oligo-directed mutagenesis Yes No No Zinc finger nucleases Yes No No*(C) (mutagenesis) Table 1, summarising ACRE‟s conclusions on the individual techniques described in this advice and the organisms produced by them. The third column shows that organisms generated during intermediate steps in the process/technique may have a different status to organisms generated at the end of the process. The latter are dealt with in the final column and are organisms that regulators, responsible for the deliberate release of GMOs, are likely to have to take a view on. Intermediate organisms may have a different status to their offspring in cases where the intermediate organism contains a transgene but selected offspring do not (e.g. reverse breeding and RNA-dependent DNA methylation). * the asterisk shows where there is uncertainty about the legal interpretation of the definition, which affects ACRE‟s conclusion on the status of the technique and/or the organisms produced by a technique. The bracketed letters (A, B or C) link this uncertainty to one of the three issues identified earlier in this summary. ACRE is concerned by the extent to which the definition of a GMO is open to interpretation. We advise that a transparent, scientifically robust interpretation be adopted if the EU continues to employ the current definition. In particular, ACRE advises that the changes conferred by these techniques are considered in the context of the extensive genetic and epigenetic variation that is present in organisms of the same species. The extent of the plasticity of plant genomes and epigenomes (and the epi/genomes of other organisms) is becoming increasingly apparent as the analytical technology in this area advances. ACRE has not been asked to consider definitions adopted in other legislative instruments and protocols. Different definitions and approaches to regulation will lead to different outcomes as to whether an organism is considered GM or not. ACRE advises that this should be taken into account when assessing the consequences of including or exempting a technique or excluding the products of a GM technique. Structure of the advice: 1. Introduction 2. Legislation 3. Cisgenics 3 4. Reverse Breeding 5. Agroinfiltration 6. Grafting on genetically modified rootstock 7. RNA-dependent DNA methylation via RNAi/siRNA 8. Oligonucleotide-Directed Mutagenesis 9. Zinc finger nucleases 10. Conclusions References 1. Introduction In 2007 the EU Commission and Member States agreed to establish an expert working group on „New Techniques‟. This was in response to an increasing number of enquiries concerning the status of products generated by techniques that regulators had not considered previously. The group finalised its report at the beginning of 20124. The EU working group was mandated to consider the status of these techniques in line with the definitions used in EU Directives dealing with the regulation of the deliberate release (Directive 2001/18 EC) and contained use (Directive 2009/41/EC) of GMOs and GMMs respectively. It was not asked to consider equivalent definitions adopted in other legislative instruments and protocols. Different definitions and approaches to regulation will lead to different outcomes as to whether an organism is considered GM or not. This should be taken into account when assessing the consequences of including or exempting a technique or excluding the products of a GM technique. For example, the UK is a signatory to the Cartegena Protocol on Biodiversity, which has a different definition of a GMO (referred to as a Living Modified Organism in this context) to that of Directive 2001/18/EC. ACRE has been requested to provide advice that will prepare UK Ministers for discussions that will ensue at EU-level. ACRE has been asked to consider the techniques that the working group is discussing and to advise Ministers on the science surrounding whether the techniques (and the organisms they generate) are captured, and on arguments for and against their regulation under the GMO legislation. While it is the role of decision-makers to interpret the legislation, it is important that ACRE advises, where appropriate, on the scientific terms used 4 This is document will not be published until it has been discussed by competent authorities under the GMO contained use and deliberate release Directives. 4 in the legislation, not only where they apply to a technique, but also where there is uncertainty and scientifically credible options open to regulators. ACRE has focused its attention on the use of the techniques as tools in plant breeding. The EU working group is also considering techniques that might fall under the scope of Directive 2009/41/EC (which concerns the contained use of GM microorganisms). The definitions and examples of GM and non-GM techniques in this legislation are very similar to those in Directive 2001/18/EC. However, there are differences: in particular, the contained use legislation excludes microorganisms produced by self-cloning (cisgenesis) as long as the resulting microorganisms are unlikely to cause disease5, whereas self-cloning is not excluded in the deliberate release legislation. The aim of plant breeding is to take advantage of existing genetic variation or to generate variation from which desirable characteristics can be selected. As the technology has advanced, the tendency is for breeders to introduce more targeted/precise changes to plant genomes and to be able to identify desirable genotypes more rapidly. Breeding techniques involving recombinant nucleic acids have also advanced since the EU‟s GMO legislation was drafted in the late 1980s (and came into force in 1990).
Details
-
File Typepdf
-
Upload Time-
-
Content LanguagesEnglish
-
Upload UserAnonymous/Not logged-in
-
File Pages44 Page
-
File Size-